Breast Cancer
Conditions
Keywords
breast cancer, ribociclib
Brief summary
This document outlines an investigator-initiated Phase Ib/II clinical trial in Japan, focusing on the combination therapy of ribociclib and anastrozole for patients with hormone receptor-positive (HR-positive), HER2-negative metastatic or recurrent breast cancer. The trial aims to evaluate the efficacy (specifically, overall response rate) and safety of this combination in the Japanese patient population. Nagoya City University is the sponsor of this trial, with funding provided by Novartis Pharma K.K.. Study Design and Endpoints: The trial is structured into two parts: * Phase Ib: The primary endpoint for this phase is tolerability, which is assessed by dose-limiting toxicities (DLT). Secondary endpoints include pharmacokinetics (PK) of the drugs, as well as the incidence of adverse events (AE) and serious adverse events (SAE). * Phase II: The primary endpoint for Phase II is the Overall Response Rate (ORR), which will be determined by a blinded central imaging review based on RECIST version 1.1 criteria. Secondary endpoints encompass PK (for the initial 20 patients), ORR as assessed by the investigator, progression-free survival (PFS), overall survival (OS), and the overall incidence of adverse events
Interventions
DRUGRibociclib 400mg
phase 1b cohort 1
DRUGRibociclib 600mg
Phase 1b cohort 2
Sponsors
Novartis
Nagoya City University
Study design
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Histologically confirmed invasive breast cancer. * Hormone receptor-positive (ER positive and/or PgR positive) and HER2-negative disease: ER positive: ≥1% positive cells or Allred score ≥3. PgR positive: ≥1% positive cells or Allred score ≥3. HER2 negative: IHC 0, 1+, or 2+ with no ISH amplification. * Advanced or recurrent breast cancer (unresectable, recurrent, or Stage IV). * Age ≥18 years at registration. * ECOG Performance Status of 0-1.
Exclusion criteria
* Symptomatic visceral metastases or deemed unsuitable for endocrine therapy. * Prior endocrine therapy or chemotherapy for metastatic/recurrent disease. * Prior CDK4/6 inhibitor exposure (perioperative or metastatic setting). * Adjuvant endocrine therapy within 35 days before study start. * Active malignancy other than allowed exceptions (e.g., resected skin cancers, ≥5-year disease-free cancers). * Hypersensitivity to ribociclib, anastrozole, or their components (including soy/peanut allergy, sugar intolerances).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Phase 1b part: Dose Limiting Toxicity | From enrollment to the end of treatment at 4 weeks |
| Phase 2 part: Overall response rate | From enrollment to the end of treatment at 24 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Phase 2 part: Overall Response Rate | From enrollment to the end of treatment at 24 weeks |
| Phase 1b part: Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 | From enrollment to the end of treatment at 4 weeks |
| Phase 2 part: Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 | From enrollment to the end of treatment at 24 weeks |
| Phase 2 part: PFS | Time Frame: From enrollment to the end of treatment at 24 weeks |
| Phase 1b part: Peak Plasma Concentration (Cmax) | From enrollment to the end of treatment at 4 weeks |
Outcome results
None listed